Clinical trial

Targeting Triple-negative Breast Cancer or ER-positive, PR Positive her2 Negative by Alkaline Glucosodiene Molecules Via a Metabolic Pathway Phase I Clinical Trial

Name
Maher M.Akl, Amr Ahmed
Description
The diverse group of breast tumors known as triple-negative breast cancer (TNBC) which is lethally and deadly type of breast cancer and insensitive to endocrine therapy and HER2-targeted therapy because it lacks the expression of estrogen, progesterone, and human epidermal growth factor receptors TNBC makes up almost 15% of all invasive breast cancers, and of all breast tumor subtypes, it has the worst overall survival and the highest rate of metastatic occurrence. Cytotoxic chemotherapy is the main established systemic therapy for early and advanced TNBC disease at the moment because there is no authorized targeted therapy. Despite the fact that chemotherapy greatly improves clinical outcomes for TNBC patients, recurrence rates are still high and TNBC cancers frequently develop chemotherapeutic drug resistance ). In light of the few available therapy choices, so few choices for this subtype of breast cancer, and many cases are resistant to chemotherapy and recurrent and with a risk of high metastasis from previous literature and many experimental studies, the target of glucose environment is a promising weapon against this deadly type of breast cancer so glucose deprivation from tumor cells may cut the glucose entry as fuel to these cancer cells so this study uses a substitute energy fuel by using alkaline glucosodiene which is chemically invented by Maher M.AKL
Trial arms
Trial start
2024-01-01
Estimated PCD
2024-12-31
Trial end
2024-12-31
Status
Not yet recruiting
Phase
Early phase I
Treatment
Alkaline Glucosodiene Molecules
Toxic chemotherapeutic nutrition of cancer cells by alkaline glucosodiene molecules via targeting metabolic of cancerous tumors: a promising treatment
Arms:
a case study with TNBC or ER positive , PR positive HER2 negative ,
Size
2
Primary endpoint
the Progression-free survival (PFS)
Time Frame: 30 days after treatment
Disease-free survival (DFS)
Time Frame: 30 days after treatment
Eligibility criteria
Inclusion Criteria: * Type of patient: Female patient * Age: 18-55 years * Type of breast cancer: metastatic breast cancer hormonal or triple-negative breast cancer Exclusion Criteria: * with other co-morbidities like diabetes or hypertension * with other type of cancers * on other chemotherapy or immunotherapy or hormonal therapy
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'interventionModelDescription': 'a case study', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 2, 'type': 'ESTIMATED'}}
Updated at
2023-07-24

1 organization

1 product

1 indication